Guest blogger & Autism Super hero sibling: Culzean Giammatteo After the school year came to a close in the summer of 2013, I spent most of my time indoors, on whatever electronic device I had access to, reading. On this particular evening I was reading like I normally do and my brother, Vico, was... Continue Reading →
It’s not an #autism behavior, it is a seizure
By Simran Garcia-TACA Orange County Akshay is a fun loving, hard working, 13 year old eating machine. When Akshay was 4 yrs old, he was diagnosed with autism. The odd thing is we were really going to the neurologist’s office to talk about seizures. I guess that’s what happens when you have to wait almost... Continue Reading →
15 years later, ready for #autism answers
By Melanie Sanchez - TACA Mom My son Andrew is 15 1/2 years old. He is non verbal, has autism, and a lovely contagious smile. He had a brief "sleep deprived" EEG done right after diagnosis when he was around 3 years old. It lasted less than an hour and hardly seemed worth the time and effort. At the... Continue Reading →
Quinn’s Trip Through Hell & Back
By Holly Riley TACA Co-coordinator Los Angeles/San Fernando Valley In May of 2005 at the age of two, my son, Quinn, was diagnosed with autism. We didn't know if he would ever speak. For that matter, we didn't know if he would ever do anything but tantrum, cover his ears and spin things in... Continue Reading →
Functional Medicine goes mainstream
By Lisa Ackerman You cannot go a day without a healthcare story being featured in the news. The Affordable Care Act, chronic health issues and access to health care have grown into one of the largest issues in American households. In the autism community, we are aware of these issues all too well. For decades,... Continue Reading →
United we stand, divided we fall
By guest blogger: Ali Hoffman – TACA Volunteer Maryland The autism community is the most divided community in the world. Some say it’s a disability, some say it’s an opportunity to celebrate diversity, and most say - that’s not my (child’s) autism. What one group does to support families is viewed as offensive to another... Continue Reading →
Max goes to the Neurologist – Part 1 of 3
By Holly Bortfeld *Disclaimer, I am a parent, not a doctor. This is not intended to be used as medical advice. If your child has a seizure, please contact a licensed physician. On the 4th of July, my son Max had a grand mal seizure. For background purposes, he’s never had seizures before. Max has... Continue Reading →
Life is what happens to you while you’re busy making other plans
By Moira Giammatteo Family Scholarship Program and Parent Mentor Program Manager When you think that you have things under control that is when something hits the fan. Five years ago we had three seizure events in our house. Vico had three grand mal seizures at age 11. One resulting in a nice scar on the... Continue Reading →